Annealing effects on the magnetization of Co–Ni–B amorphous nanoparticles

Chemically prepared (Co_xNi_1−x)_1−yB_y (x=0.5, 0.75, 1; y≈0.4) amorphous fine particles were characterized by X-ray diffraction, DTA and TGA, and in situ magnetic measurement as a function of annealing temperature in an inert atmosphere. Magnetic measurement performed in as-prepared and 150°C annealed samples shows an increase of the saturation magnetization and magnetic moment after thermal treatment. Room temperature magnetization increases by factors of 3.5, 1.8, and 1.5, for x=0.5, 0.75, and 1, respectively. These measurements may indicate a local re-ordering of the amorphous phase at temperatures much lower than the full crystallization temperature.     

Photon interaction studies using 241Am γ-rays

We have carried out some photon interaction measurements using 59.54 keV γ-rays from a ²⁴¹Am source. These include γ attenuation studies as well as photoelectric absorption studies in various samples. The attenuation studies have been made using leaf and wood samples, samples like sand, sugar etc., which contain particles of varying sizes as well as pellets and aqueous solutions of rare earth compounds. In the case of the leaf and wood samples, we have used the γ-ray attenuation technique for the determination of the water content in fresh and dried samples. The variation of the attenuation coefficient with particle size has been investigated for sand and sugar samples. The attenuation studies as well as the photoelectric studies in the case of rare earth elements have been carried out on samples containing such elements whose K-absorption edge energies lie below and close to the γ-energy used. Suitable compounds of the rare earth elements have been chosen as mixture absorbers in these investigations. A narrow beam good geometry set-up was used for the attenuation measurements. A well-shielded scattering geometry was used for the photoelectric measurements. The mixture rule was invoked to extract the values of the mass attenuation coefficients for the elements from those of the corresponding compounds. The results are consistent with theoretical values derived from the XCOM package.     

A complementary thermodynamic limit for classical Coulomb matter

The canonical equilibrium measure of classical two-component Coulomb matter with regularized interactions is analyzed in a finite volume. It is shown that, in the mean-field regime, the one-particle density is inhomogeneous on a new characteristic length scale _inh. For a system ofN positive andN negative particles, _inh and the characteristic length scale of correlations _corr (=Debye screening length) are related via _inh=(2N)^1/2 _corr. The major conceptual conclusion that is drawn from this is that one needs two nontrivial complementary thermodynamic limits to define the equilibrium thermodynamics of two-component Coulomb systems. One of them is the standard thermodynamic limit (infinite volume), where one takesN, _corr fixed. Its complementary limit is characterized byN, _inh fixed, and is a finite-volume inhomogeneous mean-field limit. The most prominent new feature in the mean-field thermodynamic limit, which is absent in the standard thermodynamic limit, is an anomalous first-order phase transition where the Coulomb system explodes or implodes, respectively. The phase transition is connected with the existence of a metastable plasma phase far below the ionization temperature.     

ZnO超微粒子光催化氧化降解n-C7H16的研究

利用ZnO光催化氧化技术对气相n-C7H16进行了降解研究，考察了氧气、水燕气体积分数等因素对n-C7H16光催化氧化的影响，利用气相色谱－质谱联用仪和气相色谱仪对气相光催化反应过程中的气体组成进行了定性分析，并对主要中间产物丙醛进行了定量分析，结果发现，ZnO超微粒子光催化氧化n-C7H16的降解率较高，n-C7H16绝大部分被完全氧化成CO2，探讨了n-C7H16光催化氧化反尖的动力学行为及机理。     

SARS CoV内对照RNA病毒样颗粒的构建和表达

在SARS-CoV的核酸检测方法中,由于普遍缺乏安全、稳定、特异的内对照,而不能对样品处理、反转录、扩增以及定量检测实施全程监控。构建的病毒样核蛋白颗粒内对照,能够对SARS-CoV临床检测实施监控。本文通过克隆1.7Kb大肠杆菌噬菌体MS2的装配蛋白和壳蛋白基因以及SARS冠状病毒经过突变产生的270bp内对照片断,并将这些基因连接到载体pTrc99a上表达,进行纯化、定量分析、RT-PCR检测和稳定性试验。获得SARS内对照病毒样核蛋白颗粒,在人血清和SM缓冲液中37℃稳定性可达到30天,能抵抗核糖核酸酶降解。将内对照颗粒加入临床样本中一同检测,能够对检测的全过程(样品处理、反转录和PCR)有效进行监控,与SARS-CoV没有交叉反应。研究表明制备的该病毒样核蛋白颗粒稳定、安全、可靠,可作为SARS冠状病毒RT-PCR检测、定量分析的有效内对照参考品。     

聚丙烯酰胺/醋酸铬与聚丙烯酰胺/酚醛胶态分散凝胶的纳米颗粒自组织分形结构

采用原子力显微镜 ,分别对无机交联体系聚丙烯酰胺 Cr3+ 和有机交联体系聚丙烯酰胺 酚醛胶态分散凝胶的微观结构进行了显微图像分析 .发现无论是在有机还是无机交联体系中 ,也无论聚丙烯酰胺和交联剂浓度如何变化 ,在微米尺度上最终形成的都是具有自相似性的树枝状分形图像 ,在更小尺度上则发现单个小树杈分形体都是由纳米级的颗粒紧密堆积而成 .在所研究的胶态分散凝胶体系中 ,树枝状分形结构的形成及其具体的形态取决于聚丙烯酰胺的浓度 ,而交联剂的有无及其多少只对树枝状凝胶分形的几何形态产生一定影响 .实验结果还表明纳米级 (≤ 10 0nm)的胶体颗粒构成的分形结构的凝胶其弹性模量G′比微米级的高出一个数量级 .且粒子尺度越小 ,则凝胶的力学稳定性越强     

Recyclable,non-leaching antimicrobial magnetic nanoparticles

Recyclable antimicrobial magnetic nanoparticles, Fe₃O₄@P(St-co-AcQAC), were prepared through surfactantfree seeded emulsion polymerization involving a polymerizable, hydrophobic quaternary ammonium compound (QAC). These antimicrobial magnetic nanoparticles demonstrated excellent antimicrobial activities against both Grampositive and Gram-negative bacteria, and can be reused for multiple times.     

Protein-coated β-ferric hydrous oxide particles: An electrokinetic and electrooptic study

Using microelectrophoresis and electric light scattering techniques, we investigated the adsorption characteristics, surface coverage and surface electric parameters of superstructures from two isoforms of plastocyanin, PCa and PCb, in an oxidized state adsorbed on β-ferric hydrous oxide particles. The surface electric charge and electric dipole moments of the composite particles and the thickness of the protein adsorption layer are determined in a wide pH range, at different ionic strengths and concentration ratios of PC to β-FeOOH. The adsorption of the two proteins was found to shift the particles’ isoelectric point and to alter the total electric charge and the electric dipole moments of the oxide particles to different extent. A “reversal” in the direction of the permanent dipole moment is observed at lower pH for PCb- than for PCa-coated oxide particles. Strict correlation is found between the changes in the electrokinetic charge of the composite particles and the variation in their “permanent” dipole moments. Data suggest that the adsorption of the proteins is driven by electrostatic and/or hydrophobic interactions with the oxide surfaces dependent on pH. The adsorption behaviour is consistent with the involvement of the “eastern” and “northern” patches of the plastocyanin molecules in their adsorption on the oxide surfaces that are differently charged depending on pH.     

Structure of polynuclear palladium(ii) hydroxocomplexes formed upon alkaline hydrolysis of palladium(ii) chloride complexes

The structure of polynuclear Pd^II hydroxocomplexes (PHC) formed as a result of alkaline hydrolysis of Pd^II chloride complexes was studied by EXAFS, SAXS, and TEM methods. It is established that in aqueous solutions a hydroxocomplex particle is a filament curled into a ball containing about 100 Pd atoms. The filament consists of planar coordination squares of PdO₄ units linkedvia one or two oxygen bridges of different geometry. Aging of samples results in an increase in the number of single bridging ligands and a decrease in the diameter of particles. Interatomic distances around palladium atoms were determined.Translated fromIzvestiya Akademii Nauk. Seriya Khimlcheskaya, No. 10, pp. 1901–1905, October, 1995.     

Growth Mechanism of Large Monodispersed Silica Particles Prepared from Tetraethoxysilane in the Presence of Sodium Dodecyl Sulfate

Monodispersed silica particles up to ca. 1.2 μm in diameter were prepared by hydrolysis of tetraethoxysilane in the presence of sodium dodecyl sulfate (SDS). The particle size was increased with an increase of SDS added. The geometrical standard deviation of the particles was decreased with an increase of SDS. In the earlier reaction stage, double spherical particles by the coalescence of the particles were frequently observed when large amounts of SDS were added. Particle size was gradually increased after the coalescence occurred and spherical particles were finally obtained. The results of Nielsen’s chronomal analysis suggest that the polynuclear layer growth took place after the coalescence of the particles in the presence of larger amount of SDS.